Organic electroluminescent device

An organic electroluminescent device having the hole-transport layer in which the hole-transport material is dispersed in the resin binder having a glass transition temperature of not less than 170.degree. C.Since the above organic electroluminescent device has the hole-transport layer exhibiting sufficient durability and higher hole-transport property, it is excellent in luminous efficiency, luminance and stability.

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Claims

1. An organic electroluminescent device having a hole-transport layer, which is formed by applying and drying a coating solution in which a hole-transport material and a resin binder having a glass transition temperature of not less than 170.degree. C. are dissolved in a solvent from which dissolved gas is previously removed.

2. An organic electroluminescent device according to claim 1, wherein the resin binder is at least one member selected from the group consisting of a polyethersulfone having a repeating unit of the formula: ##STR11## and a polysulfone having a repeating unit of the formula: ##STR12##

3. An organic electroluminescent device according to claim 1, wherein the hole-transport material is an N,N'-diphenyl-N,N'-bis(3-methylphenyl)-1,1'-biphenyl-4,4'-diamine of the formula: ##STR13##

4. An organic electroluminescent device according to claim 1, wherein the hole-transport material is present in an amount of 40 to 60% by weight with respect to an entire hole-transport layer.

5. An organic electroluminescence device according to claim 1, further including an electro-transport layer formed by depositing by vacuum deposition an electron-transport material onto the hole-transport layer.

6. An organic electroluminescence device according to claim 5, wherein the electron-transport material constituting the electron-transport layer is a tris(8-quinolinolato)aluminum (III) complex of the formula: ##STR14##

7. An organic electroluminescent device comprising:

a hole-transport layer having a layer structure that a hole-transport material is dispersed in a resin binder having a glass transition temperature of not less than 170.degree. C.; and
an electron-transport layer which is formed by depositing by vacuum deposition an electron-transport material onto the hole-transport material onto the hole-transport layer.

8. An organic electroluminescent device according to claim 7, wherein

the resin binder constituting the hole-transport layer is at least one member selected from the group consisting of a polyethersulfone having a repeating unit of the formula: ##STR15## and a polysulfone having a repeating unit of the formula: ##STR16## the hole-transport material is an N,N'-diphenyl-N,N'-bis(3-methylphenyl)-1,1'-biphenyl-4,4'-diamine of the formula: ##STR17## the electron-transport material constituting the electron-transport layer is a tris(8-quinolinolato)aluminum (III) complex of the formula: ##STR18##

9. An organic electroluminescent device according to claim 7, wherein the hole-transport material is present in an amount of 40 to 60% by weight with respect to the entire hole-transport layer.

10. An organic electroluminescence device having a hole-transport layer in which a hole-transport material and at least one fluorescent dye are dispersed in a resin binder having a glass transition temperature of not less than 170.degree. C.

11. An organic electroluminescent device according to claim 10, wherein

the resin binder constituting the hole-transport layer is at least one member selected from the group consisting of a polyethelsulfone having a repeating unit of the formula: ##STR19## and a polysulfone having a repeating unit of the formula: ##STR20## the hole-transport material is an N,N'-diphenyl-N,N'bis(3-methylphenyl)-1,1'-biphenyl-4,4'-diamine of the formula: ##STR21##

12. An organic electroluminescent device according to claim 10, wherein the hole-transport material is present in an amount of 40 to 60% by weight with respect to the entire hole-transport layer.

13. An organic electroluminescent device according to claim 10, wherein

(a) a tetraphenylbutadiene of the formula: ##STR22## (b) a coumarine 6 of the formula: ##STR23## (c) a 4-dicyanomethylene-2-methyl-6-p-dimethylaminostyryl-4H-pyran of the formula: ##STR24## are employed with respect to the fluorescent dye.

14. An organic electroluminescent device according to claim 10, wherein a first electron-transport layer composed of an electron-transport material excellent in hole-blocking property and a second electron-transport layer composed of an electron-transport material are laminated in this order on the hole-transport layer.

15. An organic electroluminescent device according to claim 14, wherein the electron-transport material for the first electron-transport layer is a triazole compound of the formula: ##STR25## and the electron-transport material for the second electron-transport layer is a tris(8-quinolinolato)aluminum (III) complex of the formula: ##STR26##

Referenced Cited
U.S. Patent Documents
5232800 August 3, 1993 Pavlisko et al.
5346752 September 13, 1994 Sawada et al.
5427858 June 27, 1995 Nakamura
5504183 April 2, 1996 Shi et al.
5505985 April 9, 1996 Nakamura
Foreign Patent Documents
2-242879 September 1990 JPX
4-85389 March 1992 JPX
5-8346 February 1993 JPX
5-25473 February 1993 JPX
5-152072 June 1993 JPX
5-194943 August 1993 JPX
6-122277 May 1994 JPX
6-290268 October 1994 JPX
7-58363 March 1995 JPX
Other references
  • Japanese J. Appl. Physical, vol. 31, (1992, pp. 960-962, Part 2, No. 7B, Jul. 15, 1992 entitled "Molecularly Doped Polymers as a Hole Transport Layer in Organic Electroluminescent Devices" by Kido et al.
Patent History
Patent number: 5821003
Type: Grant
Filed: Sep 20, 1996
Date of Patent: Oct 13, 1998
Assignee: Sumitomo Electric Industries, Ltd. (Osaka)
Inventors: Takashi Uemura (Osaka), Hiroya Kimura (Osaka), Nobuyuki Okuda (Osaka), Yoshinobu Ueba (Osaka), Yasuko Okuda (Osaka), Hajime Osaka (Osaka)
Primary Examiner: Charles Nold
Law Firm: Beveridge, DeGrandi, Weilacher & Young, L.L.P.
Application Number: 8/716,871
Classifications